메뉴 건너뛰기




Volumn 110, Issue 5, 2011, Pages 1150-1151

Necessary advances in exercise genomics and likely pitfalls

Author keywords

[No Author keywords available]

Indexed keywords

PROTEOME;

EID: 79956143373     PISSN: 87507587     EISSN: 15221601     Source Type: Journal    
DOI: 10.1152/japplphysiol.00172.2011     Document Type: Editorial
Times cited : (11)

References (10)
  • 1
    • 38349032004 scopus 로고    scopus 로고
    • Successful design and conduct of genome-wide association studies
    • Amos CI. Successful design and conduct of genome-wide association studies. Hum Mol Genet 16: R220-R225, 2007.
    • (2007) Hum Mol Genet , vol.16
    • Amos, C.I.1
  • 2
    • 79956077552 scopus 로고    scopus 로고
    • Genomic predictors of maximal oxygen uptake response to standardized exercise training programs
    • December 23, doi:10.1152/japplphysiol.00973.2010
    • Bouchard C, Sarzynski MA, Rice TK, Kraus WE, Church TS, Sung YJ, Rao DC, Rankinen T. Genomic predictors of maximal oxygen uptake response to standardized exercise training programs. J Appl Physiol (December 23, 2010). doi:10.1152/japplphysiol.00973.2010.
    • (2010) J Appl Physiol
    • Bouchard, C.1    Ma, S.2    Rice, T.K.3    Kraus, W.E.4    Church, T.S.5    Sung, Y.J.6    Rao, D.C.7    Rankinen, T.8
  • 4
    • 0141865517 scopus 로고    scopus 로고
    • Approaches to identify genes for complex human diseases: Lessons from Mendelian disorders
    • DOI 10.1002/humu.10259
    • Dean M. Approaches to identify genes for complex human diseases: lessons from Mendelian disorders. Hum Mutat 22: 261-274, 2003. (Pubitemid 37210852)
    • (2003) Human Mutation , vol.22 , Issue.4 , pp. 261-274
    • Dean, M.1
  • 7
    • 55549147191 scopus 로고    scopus 로고
    • Personal genomes: The case of the missing heritability
    • Maher B. Personal genomes: the case of the missing heritability. Nature 456: 18-21, 2008.
    • (2008) Nature , vol.456 , pp. 18-21
    • Maher, B.1
  • 8
    • 35848970794 scopus 로고    scopus 로고
    • Erratum: Genome-wide association scanning highlights two autophagy genes, ATG16L1 and IRGM, as being significantly associated with Crohn's disease (Autophagy)
    • Massey DC, Parkes M. Genome-wide association scanning highlights two autophagy genes, ATG16L1 and IRGM, as being significantly associated with Crohn's disease. Autophagy 3: 649-651, 2007. (Pubitemid 350060072)
    • (2007) Autophagy , vol.3 , Issue.6 , pp. 649-651
    • Massey, D.C.O.1    Parkes, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.